Sobbrio G A, Granata A, D'Arrigo F, Arena D, Panacea A, Trimarchi F, Granese D, Pullè C
Instit. of Clinica Medica I, University of Messina, School of Medicine, Italy.
Acta Eur Fertil. 1990 May-Jun;21(3):139-41.
In order to evaluate the clinical and endocrinological efficacy of two low-dose oral contraceptives (OC) containing 30 micrograms Ethinylestradiol (EE) and 150 micrograms Desogestrel (DG) and 75 micrograms Gestodene (GD), respectively, an open randomized study was carried out in 34 young hirsute women, matched for body mass index and age. All of them met endocrine and ultrasonic criteria for Micropolycystic Ovary Syndrome (MPCO). The participants were randomly assigned to one of two pill groups (each of 17). The serum values for Total Testosterone (TT), Free Testosterone (FT), Androstenedione (A), Dehydroepiandrosterone (DHEA), Dehydroepiandrosterone Sulphate (DHEAS), 17-Hydroxyprogesterone (17Pg), Sex Hormone Binding Globulin (SHBG), Ceruloplasmin (CP), as well as Ferriman-Gallwey Index (FGI) and Free Androgen Index (FAI) were evaluated prior to and after EE-DG and EE-GD 6 cycle treatment. A significant decrease in TT, FT, A, 17Pg, DHEA, DHEAS, FGI, FAI was observed, SHRG and CP increased significantly. There were no significant differences between the two OC. Our results seem to indicate that both OC are equipotent as far as their pharmacological profile and residual androgenic activity are concerned. Therefore, these OC may represent a highly effective and suitable alternative to the treatment of hyperandrogenism related to MPCO.
为了评估两种分别含有30微克炔雌醇(EE)和150微克去氧孕烯(DG)以及75微克孕二烯酮(GD)的低剂量口服避孕药(OC)的临床和内分泌疗效,对34名年龄和体重指数匹配的年轻多毛女性进行了一项开放性随机研究。所有受试者均符合微多囊卵巢综合征(MPCO)的内分泌和超声标准。参与者被随机分配到两个药丸组之一(每组17人)。在接受EE - DG和EE - GD 6个周期治疗之前和之后,评估总睾酮(TT)、游离睾酮(FT)、雄烯二酮(A)、脱氢表雄酮(DHEA)、硫酸脱氢表雄酮(DHEAS)、17 - 羟孕酮(17Pg)、性激素结合球蛋白(SHBG)、铜蓝蛋白(CP)的血清值,以及费里曼 - 盖尔维指数(FGI)和游离雄激素指数(FAI)。观察到TT、FT、A、17Pg、DHEA、DHEAS、FGI、FAI显著下降,SHRG和CP显著增加。两种口服避孕药之间没有显著差异。我们的结果似乎表明,就其药理特性和残留雄激素活性而言,两种口服避孕药具有同等效力。因此,这些口服避孕药可能是治疗与MPCO相关的高雄激素血症的一种高效且合适的替代方法。